Table 1.

Demographics, disease duration, and serologic profile among 2300 patients with SSc evaluated 1990–2009.

CharacteristicAge at Onset < 65 Yrs, n = 2084Age at Onset ≥ 65 Yrs, n = 216p
Women, n (%)1725 (83)184 (85)0.369
African American, n (%)379 (18)24 (11)0.040
Limited subtype disease, n (%)1302 (62)147 (68)0.108
Smoking status, current or former§992 (48)105 (50)0.601
Median no. visits to JHSC, range3 (1, 28)2 (1, 19)< 0.001
Mean followup from first visit to JHSC among patients with > 1 visit§§ (yrs, ± SD)5 ± 44 ± 3< 0.001
SSc duration, mean ± SD
  Disease duration (yrs) at time of first visit to JHSC6 ± 82 ± 3< 0.001
  Duration (yrs) of RP at time of first visit to JHSC9 ± 108 ± 130.4113
  Age of RP onset, yrs40 ± 1365 ± 13< 0.001
  Age at first non-RP symptoms, yrs43 ± 1271 ± 5< 0.001
  Years from RP onset to first non-RP SSc symptom3 ± 86 ± 13< 0.001
  Years from first non-RP SSc symptom to diagnosis of SSc by physician††2 ± 50.5 ± 2.4< 0.001
Serology, n/total analyzed (%)
  ANA1259/1306 (96)120/124 (97)0.831
  Antitopoisomerase I277/1175 (23)18/107 (17)0.112
  Anticentromere348/1288 (27)50/119 (42)0.001
  Anti-U1RNP102/1084 (9)3/99 (3)0.033
  • § Data analyzed from 2272 individuals with data recorded regarding smoking status.

  • §§ Data analyzed from 1521 individuals with > 1 visit to JHSC.

  • Data analyzed from 2227 individuals with a reported date of onset for RP.

  • †† Data analyzed from 2291 individuals with a reported date of diagnosis by a physician. SSc: systemic sclerosis (scleroderma); JHSC: Johns Hopkins Scleroderma Center; RP: Raynaud’s phenomenon; ANA: anti-nuclear antibody.